Issue 19, 2024

Ring-opening (co)polymerization of chiral seven-membered lactones mediated by achiral yttrium catalysts: insights into the catalyst stereocontrol by mass spectrometry

Abstract

Ring-opening polymerization (ROP) of cyclic esters is a preferred approach for the preparation of various polyesters with controlled microstructures. In this work, the ROP of chiral seven-membered substituted-ε-caprolactones, namely 1-methyl-ε-caprolactone (CLMe) and 1-n-butyl-ε-caprolactone (CLnBu, aka ε-decalactone), was investigated to assess the potential stereoregularity of the resulting polylactones. The reactions mediated by yttrium complexes Y{ON(N)OR2} based on non-chiral diamino-bis(o,p-disubstituted-phenolate) ligands, associated with an exogeneous alcohol as a co-initiator, were effectively catalyzed – that is, with good control over molar mass values, narrow dispersity, and chain-end fidelity. However, the tacticity of the homopolymers obtained from racemic monomers rac-CLMe or rac-CLnBu could not be evidenced by NMR spectroscopy, as outlined in previous literature reports. Alternatively, the ring-opening copolymerization (ROCOP) of equimolar mixtures of (R)-CLnBu/(S)-CLMe enabled, indirectly, the assessment of the catalyst stereocontrol through the evaluation of the ultimate degree of alternation of the inserted units of each comonomer. While NMR spectroscopy again did not enable unambiguous evaluation of the copolymer topology/sequence, detailed MALDI-ToF and high-resolution ESI mass spectrometric analyses rewardingly revealed two major series of macromolecules, cyclic and linear ones. Both series of macromolecules showed randomly distributed units of both comonomers, thereby evidencing the absence of any significant stereocontrol from the yttrium catalyst over these large, seven-membered substituted ε-caprolactones. This latter lack of stereocontrol is assumed to arise from a too long range between adjacent chiral centers, preventing an effective chain-end stereocontrolled mechanism.

Graphical abstract: Ring-opening (co)polymerization of chiral seven-membered lactones mediated by achiral yttrium catalysts: insights into the catalyst stereocontrol by mass spectrometry

Supplementary files

Article information

Article type
Paper
Submitted
27 Нау. 2024
Accepted
13 Сәу. 2024
First published
16 Сәу. 2024
This article is Open Access
Creative Commons BY-NC license

Polym. Chem., 2024,15, 1975-1991

Ring-opening (co)polymerization of chiral seven-membered lactones mediated by achiral yttrium catalysts: insights into the catalyst stereocontrol by mass spectrometry

A. Dhaini, J. Ollivier, N. Le Yondre, A. Alaaeddine, S. M. Guillaume and J. Carpentier, Polym. Chem., 2024, 15, 1975 DOI: 10.1039/D4PY00330F

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements